MODERATE RISK Terminated F-0951-2020

Benefiber Prebiotic Fiber Supplement, packaged in the following ways 1) Net Wt. 500 g (17.6 oz) bottle. UPC 886790218302 and 2) Net Wt. 760 g bottle UPC 8886790211907

Recalled by Glaxosmithkline Consumer Healthcare Holdings

Classification

Class II — Products that might cause a temporary health problem, or pose only a slight threat of a serious nature.

Fiber prebiotic product potentially contaminated with small plastic pieces

Product Quantity

170,340 bottles

Product Type

Food

Code Info

Lots: YT2Y (EXP Oct 2021), 7D6E (EXP Nov 2021), UV5C (EXP Oct 2021), 648H (EXP Nov 2021)

Voluntary/Mandated

Voluntary: Firm initiated

Distribution Pattern

Distributed to the following US states: AR, CA, FL, HI, ID, IL, LA, MA, ME, MI, MN, MO, NC, NE, NJ, NY, OH, OR, PA, RI, SC, TX, VA, WA, and WI

Company Location

Warren, NJ, 07059-6796

Report Date

05/13/2020

Recall Initiated

04/28/2020

Classification Date

05/18/2020

Termination Date

06/01/2021

Source: U.S. Food & Drug Administration (FDA) — FDA Recalls

Last updated: August 28, 2026

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